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In humans, mitochondrial DNA (mtDNA) forms closed circular molecules that contain 16,569 [4] [5] DNA base pairs, [6] with each such molecule normally containing a full set of the mitochondrial genes. Each human mitochondrion contains, on average, approximately 5 such mtDNA molecules, with the quantity ranging between 1 and 15. [ 6 ]
Human mitochondrial DNA was the first significant part of the human genome to be sequenced. [4] This sequencing revealed that human mtDNA has 16,569 base pairs and encodes 13 proteins . As in other vertebrates, the human mitochondrial genetic code differs slightly from nuclear DNA.
Each human cell contains approximately 100 mitochondria, giving a total number of mtDNA molecules per human cell of approximately 500. [35] However, the amount of mitochondria per cell also varies by cell type, and an egg cell can contain 100,000 mitochondria, corresponding to up to 1,500,000 copies of the mitochondrial genome (constituting up ...
In general, mitochondrial DNA lacks introns, as is the case in the human mitochondrial genome; [144] however, introns have been observed in some eukaryotic mitochondrial DNA, [146] such as that of yeast [147] and protists, [148] including Dictyostelium discoideum. [149] Between protein-coding regions, tRNAs are present.
The mtDNA control region is an area of the mitochondrial genome which is non-coding DNA. This region controls RNA and DNA synthesis. [1] It is the most polymorphic region of the human mtDNA genome, [2] with polymorphism concentrated in hypervariable regions. The average nucleotide diversity in these regions is 1.7%. [3]
The MT-TK gene is located on the p arm of the mitochondrial DNA at position 12 and it spans 70 base pairs. [2] The structure of a tRNA molecule is a distinctive folded structure which contains three hairpin loops and resembles a three-leafed clover .
Haplogroup T is a human mitochondrial DNA (mtDNA) haplogroup. ... These coincide with the latter part of the Andronovo period and the Saka period in the region. [5]
There is a debate concerning the geographical origins of Haplogroup M and its sibling haplogroup N. Both lineages are thought to have been the main surviving lineages involved in the out of Africa migration (or migrations) because all indigenous lineages found outside Africa belong to haplogroup M or haplogroup N. Scientists are unsure whether the mutations that define haplogroups M and N ...